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29252

Fc1ccccc1Cn1nc(-c2ncc(N3CC4CCC(C3)O4)cn2)c2cccnc21
Reaction #8683
1-(2-Fluorobenzyl)-3-[5-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-2-pyrimidinyl]-1H-pyrazolo[3,4-b]pyridine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(/C=C/CN1CC2CCC(C1)O2)N1CCc2c(sc3ncnc(Nc4cc(O)cc(Cl)c4)c23)C1
Reaction #66887
title compound
Ausbeute 38.3%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nccc(N2CC3CCC(C2)O3)n1
Reaction #162590
3-(2-chloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane
Ausbeute 89.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2nccc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162591
4-[4-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)pyrimidin-2-yl]aniline
Ausbeute 82.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(N2CC3CCC(C2)O3)nc(Cl)n1
Reaction #162592
3-(2,6-dichloro-pyrimidin-4-yl)-8-oxa-3-aza-bicyclo[3.2.1]octane
Ausbeute 83.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(-c2cc(N3CC4CCC(C3)O4)nc(Cl)n2)cc1
Reaction #162593
4-[2-chloro-6-(8-oxa-3-aza-bicyclo[3.2.1]oct-3-yl)-pyrimidin-4-yl]-phenylamine
Ausbeute 16.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2nc(Cl)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162594
3-[6-chloro-2-(4-nitro-phenyl)-pyrimidin-4-yl]-8-oxa-3-aza-bicyclo[3.2.1]octane
Ausbeute 10.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1cc(N2CC3CCC(C2)O3)nc(I)n1
Reaction #162595
desired product
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2nc(Cl)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162596
title compound
Ausbeute 79.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1cc(N2CC3CCC(C2)O3)nc(-c2ccc([N+](=O)[O-])cc2)n1
Reaction #162597
title compound
Ausbeute 198.3%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(N2CC3CCC(C2)O3)nc(-c2ccc(N)cc2)n1
Reaction #162599
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2nc(N3CC4CCC(C3)O4)cc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162600
title compound
Ausbeute 39.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(-c2cc(N3CC4CCC(C3)O4)nc(N3CC4CCC(C3)O4)n2)cc1
Reaction #162602
title compound
Ausbeute 65.6%DOI: 10.6084/m9.figshare.5104873.v1
Oc1nc(Cl)cc(N2CC3CCC(C2)O3)n1
Reaction #162605
title compound
Ausbeute 221.4%DOI: 10.6084/m9.figshare.5104873.v1
Oc1nc(N2CC3CCC(C2)O3)cc(N2CC3CCC(C2)O3)n1
Reaction #162606
title compound
Ausbeute 42.0%DOI: 10.6084/m9.figshare.5104873.v1
Clc1nc(N2CC3CCC(C2)O3)cc(N2CC3CCC(C2)O3)n1
Reaction #162607
title compound
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #162608
solid
Ausbeute 61.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Nc1cc(N2CC3CCC(C2)O3)nc(Cl)n1
Reaction #162609
title compound
Ausbeute 69.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(N2CC3CCC(C2)O3)nc(O)n1
Reaction #162610
title compound
Ausbeute 85.1%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(N2CC3CCC(C2)O3)nc(Cl)n1
Reaction #162611
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1
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